Literature DB >> 20683999

Temple-Baraitser syndrome: a rare and possibly unrecognized condition.

Adeline Jacquinet1, Marion Gérard, Michael T Gabbett, Léon Rausin, Jean-Paul Misson, Björn Menten, Geert Mortier, Lionel Van Maldergem, Alain Verloes, François-Guillaume Debray.   

Abstract

Temple-Baraitser syndrome, previously described in two unrelated patients, is the association of severe mental retardation and abnormal thumbs and great toes. We report two additional unrelated patients with Temple-Baraitser syndrome, review clinical and radiological features of previously reported cases and discuss mode of inheritance. Patients share a consistent pattern of anomalies: hypo or aplasia of the thumb and great toe nails and broadening and/or elongation of the thumbs and halluces, which have a tubular aspect. All patients were born to unrelated parents and occurred as a single occurrence in multiple sibships, suggesting sporadic inheritance from a de novo mutation mechanism. Comparative genomic hybridization in Patients 1, 2 and 3 did not reveal any copy number variations. We confirm that Temple-Baraitser syndrome represents a distinct syndrome, probably unrecognized, possibly caused by a de novo mutation in a not yet identified gene.

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Year:  2010        PMID: 20683999     DOI: 10.1002/ajmg.a.33574

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN: 1552-4825            Impact factor:   2.802


  4 in total

1.  'Splitting versus lumping': Temple-Baraitser and Zimmermann-Laband Syndromes.

Authors:  Nuria C Bramswig; C W Ockeloen; J C Czeschik; A J van Essen; R Pfundt; J Smeitink; B T Poll-The; H Engels; T M Strom; D Wieczorek; T Kleefstra; H-J Lüdecke
Journal:  Hum Genet       Date:  2015-08-12       Impact factor: 4.132

2.  Two cases of Temple-Baraitser syndrome: natural history and further delineation of the clinical and radiologic phenotypes.

Authors:  Joseph J Shen
Journal:  Clin Dysmorphol       Date:  2015-04       Impact factor: 0.816

3.  Temple-Baraitser Syndrome and Zimmermann-Laband Syndrome: one clinical entity?

Authors:  André Mégarbané; Rashid Al-Ali; Nancy Choucair; Monko Lek; Ena Wang; Moncef Ladjimi; Catherine M Rose; Remy Hobeika; Yvette Macary; Ramzi Temanni; Puthen V Jithesh; Aouatef Chouchane; Konduru S Sastry; Remy Thomas; Sara Tomei; Wei Liu; Francesco M Marincola; Daniel MacArthur; Lotfi Chouchane
Journal:  BMC Med Genet       Date:  2016-06-10       Impact factor: 2.103

4.  Syndromic disorders caused by gain-of-function variants in KCNH1, KCNK4, and KCNN3-a subgroup of K+ channelopathies.

Authors:  Karen W Gripp; Sarah F Smithson; Ingrid J Scurr; Julia Baptista; Anirban Majumdar; Germaine Pierre; Maggie Williams; Lindsay B Henderson; Ingrid M Wentzensen; Heather McLaughlin; Lisette Leeuwen; Marleen E H Simon; Ellen van Binsbergen; Mary Beth P Dinulos; Julie D Kaplan; Anne McRae; Andrea Superti-Furga; Jean-Marc Good; Kerstin Kutsche
Journal:  Eur J Hum Genet       Date:  2021-02-16       Impact factor: 4.246

  4 in total

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